A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046669



Internal ID18789200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46489628..46878295hg38UCSC Ensembl
Innerchr10:46674168..47059809hg19UCSC Ensembl
Innerchr10:46094174..46479815hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38388668
hg19385642
hg18385642
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv743n100
Supporting Variantsnssv3509131
Samples
Known GenesBMS1P1, BMS1P5, FAM35BP, FRMPD2P1, GLUD1P7, GPRIN2, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046669
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer